Please use this identifier to cite or link to this item: https://doi.org/10.1021/cg300219w
DC FieldValue
dc.titleManipulating the formation of NH 4TiOF 3 mesocrystals: Effects of temperature, surfactant, and pH
dc.contributor.authorLiu, Y.
dc.contributor.authorZhang, Y.
dc.contributor.authorLi, H.
dc.contributor.authorWang, J.
dc.date.accessioned2014-10-07T09:51:40Z
dc.date.available2014-10-07T09:51:40Z
dc.date.issued2012-05-02
dc.identifier.citationLiu, Y., Zhang, Y., Li, H., Wang, J. (2012-05-02). Manipulating the formation of NH 4TiOF 3 mesocrystals: Effects of temperature, surfactant, and pH. Crystal Growth and Design 12 (5) : 2625-2633. ScholarBank@NUS Repository. https://doi.org/10.1021/cg300219w
dc.identifier.issn15287483
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/86519
dc.description.abstractThere are two main competitive processes involved in the formation of NH 4TiOF 3 mesocrystals. One leads to the assembly of individual NH 4TiOF 3 nanocrystals and the subsequent formation of NH 4TiOF 3 mesocrystals. The other converts the NH 4TiOF 3 nanocrystals into TiO 2 (anatase) nanoparticles and results in the subsequent formation of TiO 2 aggregates. Surfactant (Brij 58) molecules appear to facilitate the mesoscale assembly of NH 4TiOF 3 nanocrystals into NH 4TiOF 3 mesocrystals via the interaction of their hydrophobic tails. Elevated temperature and higher solution pH (adjusted by ammonia solution) increase the conversion rate of NH 4TiOF 3 nanocrystals into TiO 2 (anatase) nanoparticles. This conversion process reduces the amount of NH 4TiOF 3 nanocrystals available for the mesoscale assembly and consequently increases the pore volume of the resultant NH 4TiOF 3 mesocrystals. Fluorination and {001} facets affect the photocatalytic performance of the calcined products (anatase TiO 2) of the NH 4TiOF 3 mesocrystals. The present study demonstrates the key parameters that control the formation and stability of NH 4TiOF 3 mesocrystals and the photocatalytic behavior of nanocrystalline TiO 2 derived from the mesocrystals. © 2012 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/cg300219w
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1021/cg300219w
dc.description.sourcetitleCrystal Growth and Design
dc.description.volume12
dc.description.issue5
dc.description.page2625-2633
dc.description.codenCGDEF
dc.identifier.isiut000303366000062
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